1,102 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NEO DELTA SELF SAFE T, NEO DELTA SELF SAFE T, NEO DELTA SELF SAFE 1, NEO DELTA SELF SAFE 1
FDA 510(k)
FDA Class 2
·General Hospital
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR31210071·Ligature wire preformed closed .014"
TALOS®-C HA
FDA UDI
MEDITECH SPINE, LLC·B167521210070·
Invictus
FDA UDI
ALPHATEC SPINE, INC.·00190376240992·AO Quick Connect Axial Handle, Fixed with Jewel...
TALOS®-C
FDA UDI
SpineArt SA·07640375236340·STERILE TALOS®-C (HA) PEEK PLANAR IBFD
OsteoMed
FDA UDI
OSTEOMED LLC·00845694040464·PrimaLIF LLIF 7mm x 18mm Parallel Trial
MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE
FDA 510(k)
FDA Class 2
·Cardiovascular
ULTRA PRESERVE WITH ALOE VERA (GREEN) NATURAL RUBBER LATEX EXAMINATION GLOVE MADE FROM ALLOTEX AN ENZYME TREATED NATURAL
FDA 510(k)
FDA Class 1
·General Hospital
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469242·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469235·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469228·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469280·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469211·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469266·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469259·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469273·
RESERVOIR 1.8ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 20, 2013
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 26, 2014
STERLING BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·June 13, 2011
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·May 20, 2016